Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278503Generated: October 31, 2026

4,5,6-Trichloro-2-methylpyrimidine → HCID 15003621, compound

https://huagongshe.com/reaction/2278503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5,6-Trichloro-2-methylpyrimidineHCID 231054—
ReactantSodium MethoxideHCID 10942334—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15003621HCID 1500362196.8%

Reaction Conditions

Temperature5 °C

Reaction Steps

1.37 g of sodium methoxide are added to a solution of 5 g of 2-methyl-4,5,6-trichloropyrimidine in 41 ml of THF cooled to 5° C. in an ice bath. The ice bath is removed. The suspension is stirred at ambient temperature for 18 hours. The reaction medium is cooled to 5° C. in an ice bath. 20 ml of water and 100 ml of ethyl acetate are added. After settling out, the organic phase is dried over magnesium sulfate, filtered, and concentrated under reduced pressure so as to give 4.73 g of 4,5-dichloro-6-methoxy-2-methylpyrimidine in the form of a colorless oil which crystallizes, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133168B2
Source datasetuspto-grants-2015_09
ORD IDord-9879af4a3e9f413faeb4d7b3182b496b
Source noteuspto-grants-2015_09